WO2011107567A1 - System and method for monitoring time intervals during blood parameter monitoring - Google Patents
System and method for monitoring time intervals during blood parameter monitoring Download PDFInfo
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- WO2011107567A1 WO2011107567A1 PCT/EP2011/053244 EP2011053244W WO2011107567A1 WO 2011107567 A1 WO2011107567 A1 WO 2011107567A1 EP 2011053244 W EP2011053244 W EP 2011053244W WO 2011107567 A1 WO2011107567 A1 WO 2011107567A1
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/168—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body
- A61M5/172—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic
- A61M5/1723—Means for controlling media flow to the body or for metering media to the body, e.g. drip meters, counters ; Monitoring media flow to the body electrical or electronic using feedback of body parameters, e.g. blood-sugar, pressure
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
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- A—HUMAN NECESSITIES
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- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
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- A61B5/157—Devices characterised by integrated means for measuring characteristics of blood
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- A—HUMAN NECESSITIES
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- A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
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- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
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- A—HUMAN NECESSITIES
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- A61B5/150007—Details
- A61B5/150206—Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
- A61B5/150229—Pumps for assisting the blood sampling
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61B5/150206—Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
- A61B5/150236—Pistons, i.e. cylindrical bodies that sit inside the syringe barrel, typically with an air tight seal, and slide in the barrel to create a vacuum or to expel blood
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- A—HUMAN NECESSITIES
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- A61B5/150007—Details
- A61B5/150206—Construction or design features not otherwise provided for; manufacturing or production; packages; sterilisation of piercing element, piercing device or sampling device
- A61B5/150244—Rods for actuating or driving the piston, i.e. the cylindrical body that sits inside the syringe barrel, typically with an air tight seal, and slides in the barrel to create a vacuum or to expel blood
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- A—HUMAN NECESSITIES
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- A61M2205/00—General characteristics of the apparatus
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- A61M2205/6009—General characteristics of the apparatus with identification means for matching patient with his treatment, e.g. to improve transfusion security
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- A61M2230/00—Measuring parameters of the user
- A61M2230/20—Blood composition characteristics
- A61M2230/201—Glucose concentration
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M5/00—Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
- A61M5/14—Infusion devices, e.g. infusing by gravity; Blood infusion; Accessories therefor
- A61M5/142—Pressure infusion, e.g. using pumps
- A61M5/14244—Pressure infusion, e.g. using pumps adapted to be carried by the patient, e.g. portable on the body
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- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/00584—Control arrangements for automatic analysers
- G01N35/00722—Communications; Identification
- G01N35/00871—Communications between instruments or with remote terminals
- G01N2035/00881—Communications between instruments or with remote terminals network configurations
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/28—Electrolytic cell components
- G01N27/30—Electrodes, e.g. test electrodes; Half-cells
- G01N27/327—Biochemical electrodes, e.g. electrical or mechanical details for in vitro measurements
- G01N27/3271—Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2800/00—Detection or diagnosis of diseases
- G01N2800/52—Predicting or monitoring the response to treatment, e.g. for selection of therapy based on assay results in personalised medicine; Prognosis
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- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
- G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
- G16H20/17—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered via infusion or injection
Definitions
- the invention relates to a system and a method for monitoring in each case at least one blood parameter of the blood of different patients with a plurality of access devices for establishing in each case at least one access to the blood of each patient through the skin, a plurality of removal devices each for removal an amount of blood from each patient for obtaining at least one blood sample, at least one blood analyzer for analyzing the blood sample for predeterminable parameters of the blood, and for generating individual blood parameter data sets, a computing means commonly used for a plurality of blood parameter data sets of different patients for calculating data sets from drug parameters the drugs to be administered to the respective patient on the basis of the individual blood parameter data sets and a plurality of delivery devices for supplying the respective medicament with d en calculated drug parameters with the preamble of claims 1 and 1 1st
- the delivery device may be an insulin delivery device or an infusion pump which adjusts the insulin value present within the bloodstream of the patient to a predeterminable level in response to a previously measured blood glucose value in the blood circulation system. keeps the patient's course.
- feeding devices for at least one nutritional value of a food directly or indirectly supplied to the blood circulation with at least one food supply device can be administered to the patient.
- Such delivery devices even when incorporated into a drug and / or nutritional delivery system, heretofore require entry of values by a physician or other clinician based on delivery by the delivery device. For example, quantity values, time intervals in which the supply is to take place, interval-type feeds, etc., can be entered as the basis for the subsequent delivery of, for example, insulin.
- This delivery is preceded by a mostly hand-drawn blood collection in the patients, which requires the interposition of clinical staff. Likewise, other clinical personnel are required who have the necessary expertise in the input functions of the delivery device, such as the infusion pump, to subsequently perform this delivery.
- the input of the dose unit is made possible with an infusion pump.
- this requires the consideration of information on the concentration of Active ingredient of the drug to be administered and the nature of the drug. Both when specifying the concentration of the active ingredient and when entering the dose unit and the conversion of those in the delivery rate so far only the main active ingredients of the drug are taken into account. This is often sufficient if only or primarily a specific drug is to be administered.
- Feeding or conveying devices for the supply of a drug solution mixture in a body are known several times.
- devices / systems having a plurality of infusion and / or syringe pumps, each of which delivers a solution of at least one specific drug to a body and thereby produces a drug-solution mixture are known.
- the infusion pumps have the properties of continuous and accurate metering of the medication in its delivery.
- the pumps are integrated in a common order system, which usually has a central control unit, an operating unit and an alarm unit.
- the data connection of several pumps and / or control units can also be combined in the context of a server. This possibly makes it possible, in an additional computer unit / medical computer, for even a two-digit number of different medicaments to be matched to a body and to be delivered precisely metered.
- the data is distributed by wire or by wireless LAN to the various infusion pumps.
- An essential point of the invention is that, in a system for monitoring at least one blood parameter of the blood from different patients having a plurality of access devices for establishing at least one access to the blood of each patient through the skin thereof, a plurality of withdrawal devices, respectively for extracting a quantity of blood from each patient to obtain at least one blood sample, at least one blood analyzer for analyzing the blood sample for predetermined blood parameters, and generating individual blood parameter data sets, one computing means commonly used for a plurality of blood parameter data sets of different patients for calculating data set drug parameters the patient to be administered drugs based on the individual blood parameter records and a plurality of feeding devices for supplying the respective drug with the be
- An allocation device is provided for the medication parameters which is assigned to each data record of the medication parameters of a patient calculated by the calculation device for assigning in each case an identification identifier for identifying a patient and / or a time segment identifier for specifying a time interval in which the blood collection took place performs. Such an allocation device is advantageously arranged within the calculation device.
- such an allocation device can be used for the fact that the blood parameter data sets, as obtained by the blood analysis device by the calculation device, reliably the correct identification code and / or the proper time-slot identifier to ensure that the resulting drug parameter data sets are sent to the correct delivery device, which may be an infusion pump for administration of insulin in response to a previously measured blood glucose level.
- the correct delivery device which may be an infusion pump for administration of insulin in response to a previously measured blood glucose level.
- each data record of the drug parameters for a patient can be transmitted in each case as a common data record or can be transmitted by the calculation device to one or more of the supply devices.
- the wireless transmission there may be physical separation from the computing device, which may be located within a common server, and the individual delivery devices, typically located as infusion pumps in various rooms of a hospital, directly on-site to the patient.
- At least one identification element generating device is preferably used so that each blood sample has the identification code and / or the time segment identifier in the form of a barcode, a data matrix code and / or transponder immediately after the blood quantity has been withdrawn and before being supplied to the blood analysis device the sampling device containing the blood sample can be assigned.
- a method for monitoring in each case at least one blood parameter of the blood of different patients has the following steps:
- an association device (1 1) in each case an identification identifier for identifying a patient and / or a time segment identifier for specifying a period of time in which the blood sampling took place, for each record of the blood analysis device (7, 9) determined parameters of the analyzed blood a patient (1 -3) are assigned (33).
- each data set of the determined parameters of the analyzed blood, together with the identification code and the time segment identifier, is transmitted as a common data record to the one or more of the feed devices (19, 20, 21) by the blood analysis device (7, 9).
- FIG. 2 shows a flowchart of the method according to the invention according to an embodiment of the invention.
- Fig. 1 the system according to the invention is shown in an embodiment of the invention in a schematic representation.
- a total of three inpatients 1, 2 and 3 are removed by means of a blood sampling system (for example a syringe
- Each patient has on his arm a bracelet 1 c, 2 c and 3 c, are arranged on the patient-specific data, for example by means of a bar code, a data matrix code or a transponder. These can be, for example, the identifiers of the patient.
- these sample containers e.g., syringe
- a blood analyzer 7 in accordance with the illustrated transport paths 4, 5 and 6.
- the identifiers on the wristband 1 c, 2 c and 3 c of the patient 1, 2, 3 are read out by means of a bar code or data matrix code reader 26 or a reading unit for transponders and by means of a bar code or data matrix code Generating means 25 or by means of a writing unit for transponders a corresponding barcode or a data matrix code printed or described a transponder.
- This barcode or data matrix code or transponder is adhered to the outside of the respective sample containers (e.g., syringe).
- these bar codes, data matrix codes and / or the transponder are read out by means of a reading unit 7a and at the same time the blood samples are entered into the blood analysis device.
- the blood parameter data sets created by the analysis unit are transmitted by means of a common line 10 to a receiving unit 1 1 of a calculation device 15 without wires or conducted.
- This receiving unit also receives - as shown by reference numeral 8a - data to the identification identifier and the time slot identifier.
- Both the identification identification data and the time-slot identification data and the blood parameter data records are forwarded by the receiving unit 1 1 to the calculation unit 12, which calculates, from the transmitted blood parameter data sets, drug parameter data sets which are to be determined for administering the medicaments.
- the calculation unit 12 forwards the calculated drug parameter data sets to an assignment device 13 which is suitable for associating with each calculated medication parameter data set one of the transmitted identification identifications and / or time segment identifications.
- a transmission of the common data sets, each composed of a data set of the calculated drug parameters and an identification code and / or a time segment identifier, is then transmitted on the basis of the identification code and the associated time-dependent identifier associated feeders 19, 20 and 21 which are used as infusion pumps pen as a medicament, for example insulin, the respective associated patient 1, 2, 3 administer, this is represented by the reference numerals 22, 23 and 24.
- step 33 After analyzing the blood sample according to step 32, a transfer of blood parameter data sets resulting from the analysis of the blood groups to the calculation device takes place in step 33.
- data sets of the drug parameters for the respective blood parameter data sets are calculated in accordance with step 34, in order subsequently to have an assignment of the identification code and the time segment identifier to the respective data records of the medication parameters for generating common data records in step 35.
- step 37 After transfer of the respective common data set to the associated infusion pump according to step 36, administration of the drug, step 37 takes place.
- Reference numeral 38 shows that, after a predeterminable period of time, a blood withdrawal according to step 30 takes place and thus a closed circuit exists.
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Abstract
Description
System und Verfahren für eine Datenübertragung bei der Ermittlung von System and method for data transmission in the determination of
Medikamentenparametern medications parameters
Beschreibung description
Die Erfindung betrifft ein System und ein Verfahren zur Überwachung von jeweils mindestens einem Blutparameter des Blutes von verschiedenen Patienten mit einer Mehrzahl an Zugangseinrichtungen zum Aufbau von jeweils mindestens einem Zugang zum Blut von je- dem Patienten durch dessen Haut, einer Mehrzahl an Entnahmeeinrichtungen jeweils zum Entnehmen einer Blutmenge von jedem Patienten zum Erhalten von jeweils mindestens einer Blutprobe, mindestens einer Blutanalyseeinrichtung zum Analysieren der Blutprobe hinsichtlich vorbestimmbarer Parameter des Blutes und zur Erzeugung von einzelnen Blutparameterdatensätzen, einer für eine Mehrzahl an Blutparameterdatensätzen verschiedener Patienten gemeinsam verwendbare Berechnungseinrichtung zum Berechnen von Datensätzen an Medikamentenparametern der den jeweiligen Patienten zu verabreichenden Medikamente auf Basis der einzelnen Blutparameterdatensätze und einer Mehrzahl an Zuführeinrichtungen zum Zuführen des jeweiligen Medikamentes mit den berechneten Medikamentenparametern mit dem Oberbegriff der Patentansprüche 1 und 1 1 . The invention relates to a system and a method for monitoring in each case at least one blood parameter of the blood of different patients with a plurality of access devices for establishing in each case at least one access to the blood of each patient through the skin, a plurality of removal devices each for removal an amount of blood from each patient for obtaining at least one blood sample, at least one blood analyzer for analyzing the blood sample for predeterminable parameters of the blood, and for generating individual blood parameter data sets, a computing means commonly used for a plurality of blood parameter data sets of different patients for calculating data sets from drug parameters the drugs to be administered to the respective patient on the basis of the individual blood parameter data sets and a plurality of delivery devices for supplying the respective medicament with d en calculated drug parameters with the preamble of claims 1 and 1 1st
Herkömmlicherweise werden Patienten, die insbesondere auf der Intensivstation liegen, mit Medikamenten und gegebenenfalls künstlicher Nahrung mittels einer oder mehrerer Zuführeinrichtungen, beispielsweise intravenös oder mittels Magensonde, versorgt. Beispielsweise kann die Zuführeinrichtung eine Insulinzuführeinrichtung bzw. eine Infusionspumpe sein, die den innerhalb des Blutkreislaufes des Patienten vorhandenen Insulinwert auf ein vorbestimmbares Niveau in Reaktion auf einen zuvor gemessenen Blutglukosewert im Blutkreis- lauf des Patienten hält. Ebenso können Zuführeinrichtungen für mindestens einen Nahrungswert einer mit mindestens einer Nahrungszuführeinrichtung dem Blutkreislauf direkt oder indirekt zugeführten Nahrung dem Patienten verabreicht werden. Derartige Zuführeinrichtungen, auch wenn sie in ein System zur Verabreichung von Medikamenten und/oder Nahrungswerten integriert sind, erfordern bisher die durch einen Arzt oder ein weiteres klinisches Personal zu erfolgende Eingabe von Werten, die der Zuführung mittels der Zuführeinrichtung zugrunde liegen. Beispielsweise können hier Mengenwerte, Zeitabstände, in welchen die Zuführung erfolgen soll, intervallartige Zuführungen, etc als Basis für die anschließend zu erfolgende Zuführung von beispielsweise Insulin eingegeben werden. Conventionally, patients who are particularly in the intensive care unit, supplied with drugs and possibly artificial food by means of one or more delivery devices, such as intravenous or by gavage. For example, the delivery device may be an insulin delivery device or an infusion pump which adjusts the insulin value present within the bloodstream of the patient to a predeterminable level in response to a previously measured blood glucose value in the blood circulation system. keeps the patient's course. Likewise, feeding devices for at least one nutritional value of a food directly or indirectly supplied to the blood circulation with at least one food supply device can be administered to the patient. Such delivery devices, even when incorporated into a drug and / or nutritional delivery system, heretofore require entry of values by a physician or other clinician based on delivery by the delivery device. For example, quantity values, time intervals in which the supply is to take place, interval-type feeds, etc., can be entered as the basis for the subsequent delivery of, for example, insulin.
Dieser Zuführung vorausgehend ist eine zumeist von Hand durchgeführte Blutentnahme bei den Patienten, welche die Zwischenschaltung von klinischem Personal erfordert. Ebenso ist weiteres klinisches Personal erforderlich, welches die notwendigen Fachkenntnisse zu den Eingabefunktionen der Zuführeinrichtung, wie der Infusionspumpe hat, um anschließend diese Zuführung durchzuführen. This delivery is preceded by a mostly hand-drawn blood collection in the patients, which requires the interposition of clinical staff. Likewise, other clinical personnel are required who have the necessary expertise in the input functions of the delivery device, such as the infusion pump, to subsequently perform this delivery.
Häufig ergibt sich hieraus das Problem, dass durch die Zwischenschaltung des klinischen Personals fehlerhafte Vorgehensweisen stattfinden. Beispielsweise ist es denkbar, dass eine Blutprobe dem falschen Patienten zugeordnet wird und somit die Gefahr der Verabreichung falscher Medikamente sowohl bei der Eingabe von Daten in die Zuführeinrichtung als auch bei der Blutentnahme und auch bei der Durchführung einer Blutanalyse besteht. Hinzu kommt, dass derartige Zuführeinrichtungen, wie Infusionspumpen, eine Förderrate aufweisen, die als Volumen pro Zeiteinheit (ml/h) dargestellt ist. Dem gegenüber wird in der Medizin für eine zugeführte Medikamentenlösung die Dosiseinheit verwendet. Demzufolge ist es erforderlich, dass die Dosiseinheit in eine Förderrate der Pumpe umgerechnet wird, welches die Aufgabe des behandelnden Arztes ist. Nachteilhaft bei einer derartigen Umrech- nung können häufig Rechenfehler sein, die zu Falscheingaben der Förderrate und damit zu einer unrichtigen Verabreichung von Insulin für den Patienten führt. Often this results in the problem that take place through the interposition of clinical staff incorrect procedures. For example, it is conceivable that a blood sample is assigned to the wrong patient and thus there is the risk of the administration of wrong medicines both when entering data into the delivery device and when taking blood and also when carrying out a blood analysis. In addition, such delivery devices, such as infusion pumps, have a delivery rate represented as volume per unit time (ml / hr). On the other hand, in medicine, the dose unit is used for a supplied drug solution. Accordingly, it is necessary that the dosage unit be converted into a delivery rate of the pump, which is the task of the attending physician. A disadvantage of such a conversion can often be calculation errors, which leads to incorrect inputs of the delivery rate and thus to an incorrect administration of insulin for the patient.
Denkbar ist auch, dass bei einer Infusionspumpe die Eingabe der Dosiseinheit ermöglicht wird. Allerdings erfordert dies die Berücksichtigung von Angaben über die Konzentration des Wirkstoffes des zu verabreichenden Medikamentes und über die Art des Medikamentes. Sowohl bei der Angabe der Konzentration des Wirkstoffes als auch bei der Eingabe der Dosiseinheit und der Umrechnung derjenigen in die Förderrate werden bisher ausschließlich die Hauptwirkstoffe des Medikamentes berücksichtigt. Dies ist häufig ausreichend, sofern lediglich oder vorrangig ein spezifisches Medikament verabreicht werden soll. It is also conceivable that the input of the dose unit is made possible with an infusion pump. However, this requires the consideration of information on the concentration of Active ingredient of the drug to be administered and the nature of the drug. Both when specifying the concentration of the active ingredient and when entering the dose unit and the conversion of those in the delivery rate so far only the main active ingredients of the drug are taken into account. This is often sufficient if only or primarily a specific drug is to be administered.
Zuführeinrichtungen bzw. Fördervorrichtungen für die Zuführung eines Medikamenten- Lösungsgemisches in einem Körper sind mehrfach bekannt. Beispielsweise sind Vorrichtungen/Systeme mit einer Mehrzahl an Infusions- und/oder Spritzenpumpen, wovon jeder eine Lösung mindestens einem spezifischen Medikamentenwirkstoff einem Körper zuführt und hierdurch ein Medikamenten-Lösungsgemisch entsteht, bekannt. Feeding or conveying devices for the supply of a drug solution mixture in a body are known several times. For example, devices / systems having a plurality of infusion and / or syringe pumps, each of which delivers a solution of at least one specific drug to a body and thereby produces a drug-solution mixture, are known.
Derartige Infusionspumpen-Systeme werden häufig bei Patienten, die einer intensiven, medizinischen Behandlung bedürfen, verwendet. Hierbei weisen die Infusionspumpen die Ei- genschaften der kontinuierlichen und genauen Dosierung der Medikation in ihrer Zuführung auf. Um eine optimierte Abstimmung dieser Pumpen in ihrer Dosierung zu erreichen, werden die Pumpen in einem gemeinsamen Ordnungssystem integriert, welches üblicherweise eine zentrale Steuereinheit, eine Bedienungseinheit und eine Alarmierungseinheit aufweist. Die datentechnische Verbindung mehrerer Pumpen und/oder Steuereinheiten kann auch im Rahmen eines Servers zusammengefasst sein. Dies ermöglicht gegebenenfalls in einer zusätzlichen Recheneinheit/einem medizinischen Computer, dass sogar eine zweistellige Anzahl an verschiedenen Medikamenten auf einem Körper abgestimmt und genau dosiert zugeführt werden kann. Die Daten werden drahtgebunden oder per Wireless-LAN an die ver- schiedenen Infusionspumpen verteilt. Such infusion pump systems are often used in patients who require intensive medical treatment. Here, the infusion pumps have the properties of continuous and accurate metering of the medication in its delivery. In order to achieve an optimized tuning of these pumps in their dosage, the pumps are integrated in a common order system, which usually has a central control unit, an operating unit and an alarm unit. The data connection of several pumps and / or control units can also be combined in the context of a server. This possibly makes it possible, in an additional computer unit / medical computer, for even a two-digit number of different medicaments to be matched to a body and to be delivered precisely metered. The data is distributed by wire or by wireless LAN to the various infusion pumps.
Auch im Falle der Verwendung eines Servers ist häufig das Problem, dass eine richtige Zuordnung der ermittelten Medikamente mit den dazugehörigen Medikamentenparametern zu der richtigen Infusionspumpe oder Mehrzahl an Infusionspumpen, die zu dem Patienten mit den ermittelten Blutparameterwerten zugehörig ist, durch Zwischenschaltung von klinischem Personal nicht garantiert ist. Ebenso kann mittels des gemeinsamen Servers eine Vielzahl an Pumpen bzw. Fördervorrichtungen angesteuert werden, die bei verschiedenen Patienten angeordnet sind und zur Versorgung dieser verschiedenen Patienten dienen. Demzufolge ist es Aufgabe der Erfindung, ein System und ein Verfahren zur Überwachung von jeweils mindestens einem Blutparameter des Bluts von verschiedenen Patienten zur Verfügung zu stellen, bei dem eine fehlerfreie Zuordnung berechneter Medikamentenparameter zu den jeweiligen Zuführeinrichtungen sichergestellt ist. Diese Aufgabe wird systemseitig auf die Merkmale des Anspruches 1 und verfahrensseitig auf die Merkmale des Anspruches 1 1 gelöst. Also, in the case of using a server, there is often a problem that proper association of the detected drugs with the associated drug parameters to the proper infusion pump or plurality of infusion pumps associated with the patient having the determined blood parameter values is not guaranteed by the intervention of clinical personnel is. Likewise, by means of the common server, a plurality of pumps or conveying devices can be controlled, which are arranged in different patients and serve to supply these different patients. Accordingly, it is an object of the invention to provide a system and a method for monitoring in each case at least one blood parameter of the blood from different patients, in which an error-free allocation of calculated drug parameters to the respective delivery devices is ensured. This object is achieved on the system side on the features of claim 1 and the method side to the features of claim 1 1.
Ein wesentlicher Punkt der Erfindung ist es, dass bei einem System zur Überwachung von jeweils mindestens einem Blutparameter des Bluts von verschiedenen Patienten mit einer Mehrzahl an Zugangseinrichtungen zum Aufbau von jeweils mindestens einem Zugang zum Blut von jedem Patienten durch dessen Haut, einer Mehrzahl an Entnahmeeinrichtungen jeweils zum Entnehmen einer Blutmenge von jedem Patienten zum Erhalten von jeweils mindestens einer Blutprobe, mindestens einer Blutanalyseeinrichtung zum Analysieren der Blutprobe hinsichtlich vorbestimmter Parameter des Blutes und zur Erzeugung von einzelnen Blutparameterdatensätzen, einer für eine Mehrzahl an Blutparameterdatensätzen verschiedener Patienten gemeinsam verwendbare Berechnungseinrichtung zum Berechnen von Datensätzenmedikamentenparametern der dem Patienten zu verabreichenden Medikamente auf Basis der einzelnen Blutparameterdatensätze und einer Mehrzahl an Zuführeinrichtungen zum Zuführen des jeweiligen Medikamentes mit den berechneten Medikamentenpara- metern eine Zuordnungseinrichtung zur Verfügung gestellt wird, die zum Zuordnen jeweils einer Identifikationskennung zur Identifizierung eines Patienten und/oder eine Zeitabschnitts- kennung zur Angabe eines Zeitabschnittes, in dem die Blutentnahme stattfand, zu jedem Datensatz der von der Berechnungseinrichtung berechneten Medikamentenparameter eines Patienten durchführt. Eine derartige Zuordnungseinrichtung ist vorteilhaft innerhalb der Be- rechnungseinrichtung angeordnet. An essential point of the invention is that, in a system for monitoring at least one blood parameter of the blood from different patients having a plurality of access devices for establishing at least one access to the blood of each patient through the skin thereof, a plurality of withdrawal devices, respectively for extracting a quantity of blood from each patient to obtain at least one blood sample, at least one blood analyzer for analyzing the blood sample for predetermined blood parameters, and generating individual blood parameter data sets, one computing means commonly used for a plurality of blood parameter data sets of different patients for calculating data set drug parameters the patient to be administered drugs based on the individual blood parameter records and a plurality of feeding devices for supplying the respective drug with the be An allocation device is provided for the medication parameters which is assigned to each data record of the medication parameters of a patient calculated by the calculation device for assigning in each case an identification identifier for identifying a patient and / or a time segment identifier for specifying a time interval in which the blood collection took place performs. Such an allocation device is advantageously arranged within the calculation device.
Vorteilhaft kann eine derartige Zuordnungseinrichtung dafür verwendet werden, dass die Blutparameter Datensätze, wie sie von der Blutanalyseeinrichtung durch die Berechnungseinrichtung erhalten werden, zuverlässig der richtigen Identifikationskennung und/oder der richtigen Zeitabschnittskennung zugeordnet werden, um sicherzustellen, dass die sich daraus ergebenden Medikamentenparameterdatensätze der richtigen Zuführeinrichtung, welches eine Infusionspumpe zur Verabreichung von Insulin in Antwort auf einen zuvor gemessenen Blutglukosespiegel sein kann, zugesendet werden. Auf diese Weise ist ausgeschlos- sen, dass berechnete Medikamentenparameterdatensätze an die falschen Infusionspumpen übertragen werden und somit ein Patient eine falsche Verabreichung erhält, wie es beispielsweise bei Zwischenschaltung von medizinischem Personal für die Eingabe von Datensätzen an den Infusionspumpen der Fall sein kann. Zudem kann über die Zuordnung von einer Zeitabschnittskennung sichergestellt werden, dass bei der Entnahme mehrer Blutproben von dem gleichen Patienten gewährleistet ist, dass nicht vorausgegangene berechnete Medikamentenparameterdatensätze an die dem Patienten zugeordnete Infusionspumpe gesendet werden, sondern nur derjenige Medika- mentenparameterdatensatz, der zuletzt in Verbindung mit der Identifikationskennung zu dem ausgewählten Patienten berechnet worden ist. Advantageously, such an allocation device can be used for the fact that the blood parameter data sets, as obtained by the blood analysis device by the calculation device, reliably the correct identification code and / or the proper time-slot identifier to ensure that the resulting drug parameter data sets are sent to the correct delivery device, which may be an infusion pump for administration of insulin in response to a previously measured blood glucose level. In this way, it is ruled out that calculated drug parameter data sets are transferred to the wrong infusion pumps and thus a patient receives an incorrect administration, as may be the case, for example, when medical personnel are involved in the input of data sets to the infusion pump. In addition, it can be ensured via the association of a time segment identifier that, when multiple blood samples are taken from the same patient, it is possible to send non-predicted calculated drug parameter data records to the infusion pump assigned to the patient, but only that medication parameter data record that was last used in conjunction with the identifier for the selected patient has been calculated.
Vorteilhaft ist jeder Datensatz der Medikamentenparameter für einen Patienten zusammen mit der Identifikationskennung und der Zeitabschnittskennung jeweils als gemeinsamer Datensatz leitungsgebunden oder leitungslos von der Berechnungseinrichtung an eine oder mehrere der Zuführeinrichtungen übertragbar. Aufgrund der leitungslosen Übertragung kann eine räumliche Trennung von der Berechnungseinrichtung, die innerhalb eines gemeinsamen Servers angeordnet sein kann, und den einzelnen Zuführeinrichtungen, die in der Regel als Infusionspumpen in verschiedenen Zimmern eines Krankenhauses direkt vor Ort zu dem Patienten angeordnet sind, bestehen. Advantageously, each data record of the drug parameters for a patient, together with the identification code and the time segment identifier, can be transmitted in each case as a common data record or can be transmitted by the calculation device to one or more of the supply devices. Because of the wireless transmission, there may be physical separation from the computing device, which may be located within a common server, and the individual delivery devices, typically located as infusion pumps in various rooms of a hospital, directly on-site to the patient.
Mindestens eine Identifikationselementen-Erzeugungseinrichtung wird vorzugsweise dafür verwendet, dass jede Blutprobe unmittelbar nach dem Entnehmen der Blutmenge und vor dem Zuführen zu der Blutanalyseeinrichtung die Identifikationskennung und/oder die Zeitabschnittskennung in Form von einem Barcode, einem Datenmatrix-Code und/oder Transpon- der auf der die Blutprobe enthaltenden Entnahmeeinrichtung zuordenbar ist. Vorteilhaft weist ein Verfahren zur Überwachung von jeweils mindestens einem Blutparameter des Blutes von verschiedenen Patienten folgende Schritte auf: At least one identification element generating device is preferably used so that each blood sample has the identification code and / or the time segment identifier in the form of a barcode, a data matrix code and / or transponder immediately after the blood quantity has been withdrawn and before being supplied to the blood analysis device the sampling device containing the blood sample can be assigned. Advantageously, a method for monitoring in each case at least one blood parameter of the blood of different patients has the following steps:
Verfahren zur Überwachung von jeweils mindestens einem Blutparameter des Bluts von ver- schiedenen Patienten (1 , 2, 3), mit folgenden Schritten: Method for monitoring in each case at least one blood parameter of the blood of different patients (1, 2, 3), with the following steps:
- Aufbauen von jeweils mindestens einem Zugang zum Blut von jedem Patienten (1 , 2, 3) mittels einer Mehrzahl an Zugangseinrichtungen (1 a, 2a, 3a); - establishing in each case at least one access to the blood of each patient (1, 2, 3) by means of a plurality of access devices (1a, 2a, 3a);
- Entnehmen (30) einer Blutmenge von jedem Patienten (1 -3) zum Erhalten von jeweils mindestens einer Blutprobe mittels einer Mehrzahl an Entnahmeeinrichtun- gen (1 b, 2b, 3b); - withdrawing (30) a quantity of blood from each patient (1-3) for obtaining in each case at least one blood sample by means of a plurality of removal devices (1b, 2b, 3b);
- Analysieren (32) der Blutprobe hinsichtlich vorbestimmbarer Parameter des Blutes mittels einer Mehrzahl an Blutproben verschiedener Patienten (1 -3) gemeinsam - Analyzing (32) the blood sample in terms of predeterminable parameters of the blood by means of a plurality of blood samples of different patients (1-3) together
verwendbare Blutanalyseeinrichtungen (7, 9); usable blood analyzers (7, 9);
- Berechnen (35) von Medikamentenparametern der den jeweiligen Patienten zu - Compute (35) of drug parameters of the respective patients
verabreichenden Medikamenten auf Basis von Datensätzen der ermittelten administering drugs based on data sets of the determined
Parameter des analysierten Blutes mittels einer gemeinsamen Berechnungseinrichtung (15); und Parameters of the analyzed blood by means of a common calculation device (15); and
- Zuführen (37) des jeweiligen Medikamentes mit den berechneten Medikamentenparametern mittels einer Mehrzahl an Zuführeinrichtungen (19, 20, 21 ), - supplying (37) the respective medicament with the calculated medicament parameters by means of a plurality of supply devices (19, 20, 21),
wobei mittels einer Zuordnungseinrichtung (1 1 ) jeweils eine Identifikationskennung zur Identifizierung eines Patienten und/oder eine Zeitabschnittskennung zur Angabe eines Zeitabschnittes, in dem die Blutentnahme stattfand, zu jedem Datensatz der von der Blutanalyseeinrichtung (7, 9) ermittelten Parameter des analysierten Blutes einen Patienten (1 -3) zugeordnet (33) werden. wherein by means of an association device (1 1) in each case an identification identifier for identifying a patient and / or a time segment identifier for specifying a period of time in which the blood sampling took place, for each record of the blood analysis device (7, 9) determined parameters of the analyzed blood a patient (1 -3) are assigned (33).
In einem derartigen Verfahren wird jeder Datensatz der ermittelten Parameter des analysierten Blutes zusammen mit der Identifikationskennung und der Zeitabschnittskennung jeweils als gemeinsamer Datensatz leitungsgebunden oder leitungslos von der Blutanalyseeinrichtung (7, 9) an eine oder mehrere der Zuführeinrichtungen (19, 20, 21 ) übertragen. In such a method, each data set of the determined parameters of the analyzed blood, together with the identification code and the time segment identifier, is transmitted as a common data record to the one or more of the feed devices (19, 20, 21) by the blood analysis device (7, 9).
Weitere vorteilhafte Ausführungsformen ergeben sich aus den Unteransprüchen und der nachfolgenden Beschreibung in Verbindung mit der Zeichnung. Hierbei zeigen: Fig. 1 In einer schematischen Darstellung das erfindungsgemäße System gemäß einer Ausführungsform der Erfindung in seinem Funktionsablauf; und Further advantageous embodiments will become apparent from the dependent claims and the following description taken in conjunction with the drawings. Hereby show: 1 is a schematic representation of the system according to the invention according to an embodiment of the invention in its functional sequence; and
Fig. 2 In einem Flussdiagramm das erfindungsgemäße Verfahren gemäß einer Ausfüh- rungsform der Erfindung. 2 shows a flowchart of the method according to the invention according to an embodiment of the invention.
In Fig. 1 ist in einer schematischen Darstellung das erfindungsgemäße System in einer Ausführungsform der Erfindung gezeigt. Wie der Darstellung gemäß Fig. 1 zu entnehmen ist, wird bei insgesamt drei stationär liegenden Patienten 1 ,2 und 3 mittels eines Blutentnahmesystems (z.B. einer Spritze In Fig. 1, the system according to the invention is shown in an embodiment of the invention in a schematic representation. As can be seen from the illustration according to Fig. 1, a total of three inpatients 1, 2 and 3 are removed by means of a blood sampling system (for example a syringe
1 b, 2b und 3b, die jeweils eine Nadel 1 a, 2a und 3a aufweisen) Blut entnommen. 1 b, 2b and 3b, each having a needle 1 a, 2a and 3a) taken blood.
Jeder Patient hat an seinem Arm ein Armband 1 c, 2c und 3c, auf dem patientenspezifische Daten, beispielsweise mittels eines Barcodes, eines Datamatrix-Codes oder eines Transponders angeordnet sind. Dies können beispielsweise die Identifikationskennungen des Patienten sein. Each patient has on his arm a bracelet 1 c, 2 c and 3 c, are arranged on the patient-specific data, for example by means of a bar code, a data matrix code or a transponder. These can be, for example, the identifiers of the patient.
Sobald eine Blutprobe mittels des Blutentnahmesystems 1 b, 2b und 3b entnommen worden ist, werden diese Probenbehälter (z.B. Spritze) gemäß den dargestellten Transportwegen 4, 5 und 6 zu einer Blutanalyseeinrichtung 7 transportiert. Once a blood sample has been withdrawn by the blood collection systems 1b, 2b and 3b, these sample containers (e.g., syringe) are transported to a blood analyzer 7 in accordance with the illustrated transport paths 4, 5 and 6.
Zeitgleich oder zuvor werden mittels eines Barcode- oder Datamatrix-Code-Lesers 26 oder einer Leseeinheit für Transponder die Kennungen auf dem Armband 1 c, 2c und 3c des Pati- enten 1 , 2, 3 ausgelesen und mittels einer Barcode- oder Datamatrix-Code- Erzeugungseinrichtung 25 oder mittels einer Schreibeinheit für Transponder ein entsprechender Barcode oder ein Datamatrix-Code ausgedruckt bzw. ein Transponder beschrieben. Dieser Barcode bzw. Datamatrix-Code oder dieser Transponder werden auf die jeweiligen Probenbehälter (z.B. Spritze) außenseitig aufgeklebt. At the same time or beforehand, the identifiers on the wristband 1 c, 2 c and 3 c of the patient 1, 2, 3 are read out by means of a bar code or data matrix code reader 26 or a reading unit for transponders and by means of a bar code or data matrix code Generating means 25 or by means of a writing unit for transponders a corresponding barcode or a data matrix code printed or described a transponder. This barcode or data matrix code or transponder is adhered to the outside of the respective sample containers (e.g., syringe).
Bei Ankunft bei der Blutanalyseeinrichtung 7 werden diese Barcodes, Datamatrix-Codes und/oder der Transponder mittels einer Leseeinheit 7a ausgelesen und zugleich die Blutproben in die Blutanalyseeinrichtung eingegeben. Ein anschließender Datentransfer von der Leseeinheit 7 zu einer Analyseeinheit 9 innerhalb der Blutanalyseeinrichtung 7, wie er durch Bezugzeichen 8 wiedergegeben wird, führt dazu, dass die Identifikationskennung und die Zeitabschnittskennung an die Analyseeinheit und gemäß Bezugszeichen 10 an eine Zuordnungseinrichtung 1 1 weitergegeben werden, wobei zugleich innerhalb der Analyseeinheit 9 eine Analysierung der Blutprobe zur Feststellung vorbestimmbarer Blutparameter stattfindet. Upon arrival at the blood analysis device 7, these bar codes, data matrix codes and / or the transponder are read out by means of a reading unit 7a and at the same time the blood samples are entered into the blood analysis device. Subsequent data transfer from the reading unit 7 to an analysis unit 9 within the blood analyzer 7, as represented by reference numeral 8, results in the identifier and the time slot identifier being forwarded to the analyzer and, according to reference numeral 10, to an associate 1 1, at the same time within the analysis unit 9, an analysis of the blood sample for the determination of predeterminable blood parameters takes place.
Die von der Analyseeinheit erstellten Blutparameterdatensätze werden mittels einer gemeinsamen Leitung 10 an eine Empfangseinheit 1 1 einer Berechnungseinrichtung 15 leitungslos oder leitungsgebunden übertragen. Diese Empfangseinheit erhält ebenso - wie mit dem Bezugszeichen 8a dargestellt - Daten zu der Identifikationskennung und der Zeitabschnittskennung. Sowohl die Identifikationskennungsdaten als auch die Zeitabschnittskennungsdaten und die Blutparameterdatensätze werden von der Empfangseinheit 1 1 an die Berechnungseinheit 12 weitergegeben, welche aus den übermittelten Blutparameterdatensätzen Medika- mentenparameterdatensätze berechnet, welche zur Verabreichung der Medikamente zu ermitteln sind. The blood parameter data sets created by the analysis unit are transmitted by means of a common line 10 to a receiving unit 1 1 of a calculation device 15 without wires or conducted. This receiving unit also receives - as shown by reference numeral 8a - data to the identification identifier and the time slot identifier. Both the identification identification data and the time-slot identification data and the blood parameter data records are forwarded by the receiving unit 1 1 to the calculation unit 12, which calculates, from the transmitted blood parameter data sets, drug parameter data sets which are to be determined for administering the medicaments.
Anschließend leitet die Berechnungseinheit 12 die berechneten Medikamentenparameterda- tensätze an eine Zuordnungseinrichtung 13 weiter, welche dazu geeignet ist, jedem berech- neten Medikamentenparameterdatensatz eine der übermittelten Identifikationskennungen und/oder Zeitabschnittskennungen zuzuordnen. Subsequently, the calculation unit 12 forwards the calculated drug parameter data sets to an assignment device 13 which is suitable for associating with each calculated medication parameter data set one of the transmitted identification identifications and / or time segment identifications.
Zusätzlich kann mittels einer Tastatur 14a oder einer ähnlichen Eingabeeinrichtung weitere Parameter in eine Speichereinheit 14 eingegeben werden oder auch durch Kommunikation mit der Empfangseinheit 1 1 die entsprechenden übertragenen Identifikationskennungen und Zeitabschnittskennungen zu dem jeweiligen Blutparameterdatensatz geändert werden. Dies wird dann ebenso der Zuordnungseinrichtung 13 für eine richtige Zuordnung zu dem jeweils berechneten Medikamentenparameterdatensatz weiter übermittelt. Gemäß den Bezugszeichen 16, 17 und 18 findet anschließend eine Übertragung der gemeinsamen Datensätze, die sich jeweils aus einem Datensatz der berechneten Medikamentenparameter und einer Identifikationskennung und/oder einer Zeitabschnittskennung zusammensetzen, anhand der Identifikationskennung und der Zeitabschnittskennung ausgewählten zugehörigen Zuführeinrichtungen 19, 20 und 21 übertragen, die als Infusionspum- pen als Medikament, zum Beispiel Insulin, dem jeweils zugehörigen Patienten 1 , 2, 3 verabreichen, dies wird mittels der Bezugszeichen 22, 23 und 24 dargestellt. In addition, further parameters can be entered into a memory unit 14 by means of a keyboard 14a or a similar input device, or the corresponding transmitted identification identifications and time segment identifications for the respective blood parameter data set can also be changed by communication with the receiving unit 11. This is then also forwarded to the allocation device 13 for a correct assignment to the respectively calculated medication parameter data record. 16, 17 and 18, a transmission of the common data sets, each composed of a data set of the calculated drug parameters and an identification code and / or a time segment identifier, is then transmitted on the basis of the identification code and the associated time-dependent identifier associated feeders 19, 20 and 21 which are used as infusion pumps pen as a medicament, for example insulin, the respective associated patient 1, 2, 3 administer, this is represented by the reference numerals 22, 23 and 24.
In dem Flussdiagramm gemäß Fig. 2 wird ein Verfahren gemäß einer Ausführungsform der Erfindung gezeigt. In the flowchart of FIG. 2, a method according to an embodiment of the invention is shown.
Dieser Darstellung ist zu entnehmen, dass in einem anfänglichen Schritt 30 Blutproben von mehreren Patienten entnommen werden, die anschließend in der Blutanalyseeinrichtung eingelesen werden (Schritt 31 ). This illustration shows that, in an initial step 30, blood samples are taken from several patients, which are subsequently read in the blood analysis device (step 31).
Nach einem Analysieren der Blutprobe gemäß Schritt 32 findet in Schritt 33 eine Übertragung von Blutparameterdatensätzen, die sich aus der Analysierung der Blutgruppen ergeben, an die Berechnungseinrichtung statt. In der Berechnungseinrichtung werden Datensätze der Medikamentenparameter zu den jeweiligen Blutparameterdatensätzen gemäß Schritt 34 berechnet, um anschließend in Schritt 35 eine Zuordnung der Identifikationskennung und der Zeitabschnittskennung zu den jeweiligen Datensätzen der Medikamentenparameter zur Erzeugung von gemeinsamen Datensätzen erfolgen zu lassen. After analyzing the blood sample according to step 32, a transfer of blood parameter data sets resulting from the analysis of the blood groups to the calculation device takes place in step 33. In the calculation device, data sets of the drug parameters for the respective blood parameter data sets are calculated in accordance with step 34, in order subsequently to have an assignment of the identification code and the time segment identifier to the respective data records of the medication parameters for generating common data records in step 35.
Nach einer Übertragung des jeweils gemeinsamen Datensatzes an die zugehörige Infusionspumpe gemäß Schritt 36 findet eine Verabreichung des Medikamentes, Schritt 37 statt. After transfer of the respective common data set to the associated infusion pump according to step 36, administration of the drug, step 37 takes place.
Mit Bezugszeichen 38 wird dargestellt, dass nach einem vorbestimmbaren Zeitabschnitt wie- derum eine Blutentnahme gemäß Schritt 30 stattfindet und somit ein geschlossener Kreislauf existiert. Reference numeral 38 shows that, after a predeterminable period of time, a blood withdrawal according to step 30 takes place and thus a closed circuit exists.
Sämtliche in den Anmeldungsunterlagen offenbarten Merkmale werden als erfindungswesentlich beansprucht, sofern sie einzeln oder in Kombination gegenüber dem Stand der Technik neu sind. Bezugszeichenliste All disclosed in the application documents features are claimed as essential to the invention, provided they are new individually or in combination over the prior art. LIST OF REFERENCE NUMBERS
1 Patient 1 1 patient 1
1 a Nadel Patient 1 1 a needle patient 1
1 b Spritze Patient 1 1 b syringe patient 1
1 c Armband Patient 1 1 c patient bracelet 1
2 Patient 2 2 patient 2
2a Nadel Patient 2 2a needle patient 2
2b Spritze Patient 2 2b syringe patient 2
2c Armband Patient 2 2c bracelet patient 2
3 Patient 3 3 patient 3
3a Nadel Patient 3 3a needle patient 3
3b Spritze Patient 3 3b syringe patient 3
3c Armband Patient 3 3c bracelet patient 3
4 Transportweg 4 transport route
5 Transportweg 5 transport route
6 Transportweg 6 transport route
7 Blutanalyseeinrichtung 7 blood analysis device
7a Leseeinheit 7a reading unit
8 Datentransfer 8 data transfer
9 Analyseeinheit 9 analysis unit
10 gemeinsame Leitung 10 common line
1 1 Empfangseinheit 1 1 receiving unit
12 Berechnungseinheit 12 calculation unit
13 Zuordnungseinrichtung 13 allocation device
14 Speichereinheit 14 storage unit
14a Tastatur 14a keyboard
15 Berechnungseinrichtung 15 calculation device
16 Senden der Medikamentenparameter an die Infusionspumpe 16 Send the drug parameters to the infusion pump
17 Senden der Medikamentenparameter an die Infusionspumpe17 Send the drug parameters to the infusion pump
18 Senden der Medikamentenparameter an die Infusionspumpe18 Send the drug parameters to the infusion pump
19 Zuführeinrichtung 19 feeder
20 Zuführeinrichtung 21 Zuführeinrichtung 20 feeder 21 feeder
22 Verabreichen der richtigen Dosis des Insulins 22 Administer the right dose of insulin
23 Verabreichen der richtigen Dosis des Insulins 23 Administer the right dose of insulin
24 Verabreichen der richtigen Dosis des Insulins 24 Administer the right dose of insulin
25 Barcode- oder Datamatrix-Code-Erzeugungseinheit 25 bar code or data matrix code generation unit
26 Datamatrix-Code-Leser 26 data matrix code reader
30 Entnehmen einer Blutmenge 30 Taking a quantity of blood
31 Einlesen der Blutproben in der Blutanalyseeinrichtung 31 Reading the Blood Samples in the Blood Analyzer
32 Analysieren der Blutprobe 32 Analyzing the blood sample
33 Übertragung der Blutparameterdatensätze 33 Transmission of Blood Parameter Records
34 Berechnen der Medikamentenparameter 34 Calculating the drug parameters
35 Zuordnung der Kennungen der Medikamentenparameter 35 Assignment of the identifiers of the drug parameters
36 Übertragung der Medikamentenparameter an die Infusionspumpen 36 Transfer of the drug parameters to the infusion pumps
37 Verabreichung des Medikamentes 37 administration of the drug
38 Kreislauf des Verfahrens 38 cycle of the process
Claims
Priority Applications (12)
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| CN2011800104607A CN102804191A (en) | 2010-03-05 | 2011-03-03 | System and method for monitoring time intervals during blood parameter monitoring |
| CA2789191A CA2789191C (en) | 2010-03-05 | 2011-03-03 | System and method for monitoring time intervals during blood parameter monitoring |
| ES11707397.3T ES2655370T3 (en) | 2010-03-05 | 2011-03-03 | System for data transmission during the determination of medication parameters |
| JP2012553353A JP5658767B2 (en) | 2010-03-05 | 2011-03-03 | System for measuring blood parameters |
| BR112012020923A BR112012020923A2 (en) | 2010-03-05 | 2011-03-03 | system and method for monitoring time intervals during blood parameter monitoring. |
| MX2012009596A MX2012009596A (en) | 2010-03-05 | 2011-03-03 | System and method for monitoring time intervals during blood parameter monitoring. |
| EP11707397.3A EP2542992B1 (en) | 2010-03-05 | 2011-03-03 | System for data transmission in determination of medicament parameters |
| AU2011222943A AU2011222943B2 (en) | 2010-03-05 | 2011-03-03 | System and method for monitoring time intervals during blood parameter monitoring |
| RU2012134289/08A RU2543941C2 (en) | 2010-03-05 | 2011-03-03 | System for time slot tracking and method for time slot tracking during blood value tracking |
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| SG2012060869A SG183353A1 (en) | 2010-03-05 | 2011-03-03 | System and method for monitoring time intervals during blood parameter monitoring |
| IL221413A IL221413B (en) | 2010-03-05 | 2012-08-12 | System and method for monitoring time intervals during blood parameter monitoring |
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| PCT/EP2011/053243 Ceased WO2011107566A1 (en) | 2010-03-05 | 2011-03-03 | System for determining treatment-related data for the administration of drugs to patients to be treated taking into account important individual factors |
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| PCT/EP2011/053243 Ceased WO2011107566A1 (en) | 2010-03-05 | 2011-03-03 | System for determining treatment-related data for the administration of drugs to patients to be treated taking into account important individual factors |
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2011
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